Laura M. Watts

Du Cane Road
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 19 publications

Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis.

Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: September 16, 2025

Neuro-ophthalmic complications of endosteal hyperostosis, Worth type: the importance of ophthalmic monitoring.

Neuro-ophthalmic complications of endosteal hyperostosis, Worth type: the importance of ophthalmic monitoring.

Journal: Ophthalmic genetics

Published: August 26, 2025

The GWAS candidate far upstream element binding protein 3 (FUBP3) is required for normal skeletal growth, and adult bone mass and strength in mice.

The GWAS candidate far upstream element binding protein 3 (FUBP3) is required for normal skeletal growth, and adult bone mass and strength in mice.

Journal: Bone

Published: December 31, 2024

Biallelic FGF4 Variants Linked to Thoracic Dystrophy and Respiratory Insufficiency.

Biallelic FGF4 Variants Linked to Thoracic Dystrophy and Respiratory Insufficiency.

Journal: Clinical genetics

Published: November 24, 2024

FILIP1-associated neuromuscular disorder and phenotypic blending due to paternal UPD6.

FILIP1-associated neuromuscular disorder and phenotypic blending due to paternal UPD6.

Journal: Brain communications

Published: March 12, 2024

The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients.

The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients.

Journal: European journal of human genetics : EJHG

Published: January 18, 2024

Rare disease gene association discovery in the 100,000 Genomes Project.

Rare disease gene association discovery in the 100,000 Genomes Project.

Journal: Nature

Published: December 19, 2023

Neuropathic-like Pain in Fibrous Dysplasia/McCune-Albright Syndrome.

Neuropathic-like Pain in Fibrous Dysplasia/McCune-Albright Syndrome.

Journal: The Journal of clinical endocrinology and metabolism

Published: February 10, 2021

Rare musculoskeletal diseases in adults: a research priority setting partnership with the James Lind Alliance.

Rare musculoskeletal diseases in adults: a research priority setting partnership with the James Lind Alliance.

Journal: Orphanet journal of rare diseases

Published: March 31, 2020

The severity of ankylosing spondylitis and responses to anti-tumour necrosis factor biologics are not influenced by the tumour necrosis factor receptor polymorphism incriminated in multiple sclerosis.

The severity of ankylosing spondylitis and responses to anti-tumour necrosis factor biologics are not influenced by the tumour necrosis factor receptor polymorphism incriminated in multiple sclerosis.

Journal: Genes and immunity

Published: September 18, 2017

ERAP1 association with ankylosing spondylitis is attributable to common genotypes rather than rare haplotype combinations.

ERAP1 association with ankylosing spondylitis is attributable to common genotypes rather than rare haplotype combinations.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: January 05, 2017

Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia.

Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia.

Journal: Orphanet journal of rare diseases

Published: August 23, 2016

Showing 1-12 of 19

Last Updated: 09/26/2026